|
severe dental aberrations in familial steroid dehydrogenase deficiency
|
17904 |
|
|
Gitelman syndrome; GTLMNS
|
http://purl.obolibrary.org/obo/MONDO_0009904 |
|
|
diffuse cutaneous Leishmaniases
|
43904 |
|
|
CORNEAL DYSTROPHY, MEESMANN, 2
|
32904 |
|
|
massive macronodular adrenocortical disease
|
9049 |
|
|
disorder, chromosome abnormality
|
19040 |
|
|
claw-like fingers and toes
|
9048 |
|
|
Complex of anomalies involving the cranium and brain
|
9042 |
|
|
multiple congenital anomalies/dysmorphic syndrome
|
19042 |
|
|
alopecia, pigmentation anomaly thumb deformity
|
C536904 |
|
|
Leishmaniases, diffuse cutaneous
|
43904 |
|
|
occult squamous cell carcinoma of lung
|
3904 |
|
|
occult squamous cell carcinoma of the lung
|
3904 |
|
|
occult squamous cell lung carcinoma
|
3904 |
|
|
chromosome disorder, autosomal
|
19040 |
|
